BRPI0519316B1 - WATER HERBICIDE COMPOSITION AND PROCESS FOR PREPARING A COMPOSITION - Google Patents
WATER HERBICIDE COMPOSITION AND PROCESS FOR PREPARING A COMPOSITION Download PDFInfo
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- BRPI0519316B1 BRPI0519316B1 BRPI0519316-8A BRPI0519316A BRPI0519316B1 BR PI0519316 B1 BRPI0519316 B1 BR PI0519316B1 BR PI0519316 A BRPI0519316 A BR PI0519316A BR PI0519316 B1 BRPI0519316 B1 BR PI0519316B1
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- Prior art keywords
- composition
- surfactant
- betaine
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- weight
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 146
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 239000004009 herbicide Substances 0.000 title description 9
- 239000004094 surface-active agent Substances 0.000 claims abstract description 132
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims abstract description 124
- 229960003237 betaine Drugs 0.000 claims abstract description 63
- 238000000034 method Methods 0.000 claims abstract description 13
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical class OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 42
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 27
- 150000001412 amines Chemical class 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical group CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 8
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 6
- 150000005690 diesters Chemical class 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- 229940106681 chloroacetic acid Drugs 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 3
- 239000011149 active material Substances 0.000 claims description 3
- 239000002518 antifoaming agent Substances 0.000 claims description 3
- ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 claims description 3
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 2
- 239000004519 grease Substances 0.000 claims description 2
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 abstract description 13
- 238000002360 preparation method Methods 0.000 abstract description 5
- 150000003839 salts Chemical class 0.000 description 31
- 239000005562 Glyphosate Substances 0.000 description 24
- 229940097068 glyphosate Drugs 0.000 description 24
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- -1 alkyl betaine Chemical compound 0.000 description 14
- 239000004615 ingredient Substances 0.000 description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 7
- 239000013078 crystal Substances 0.000 description 7
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 125000006353 oxyethylene group Chemical group 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000010612 desalination reaction Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229930182470 glycoside Natural products 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- 230000000750 progressive effect Effects 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- QWCKQJZIFLGMSD-VKHMYHEASA-N L-alpha-aminobutyric acid Chemical compound CC[C@H](N)C(O)=O QWCKQJZIFLGMSD-VKHMYHEASA-N 0.000 description 1
- 244000100545 Lolium multiflorum Species 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000000245 Raphanus raphanistrum subsp raphanistrum Nutrition 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000011380 Raphanus sativus Nutrition 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-L phosphoramidate Chemical compound NP([O-])([O-])=O PTMHPRAIXMAOOB-UHFFFAOYSA-L 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- KPFSGNRRZMYZPH-UHFFFAOYSA-M potassium;2-chloroacetate Chemical compound [K+].[O-]C(=O)CCl KPFSGNRRZMYZPH-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/36—Organic compounds containing phosphorus
- C11D3/364—Organic compounds containing phosphorus containing nitrogen
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
composição aquosa herbicida, e, processo para a preparação de uma composição. a presente invenção refere-se a composições herbicidas compostas de um sal de aminofosfato ou de aminofosfonato, especialmente a composições herbicidas compostas de uma quantidade relativamente elevada de um sal de aminofosfato ou de aminofosfonato e uma composição tensoativa baseada em betaína de matéria.herbicidal aqueous composition, and process for the preparation of a composition. The present invention relates to herbicidal compositions composed of an aminophosphate or aminophosphonate salt, especially to herbicidal compositions composed of a relatively high amount of an aminophosphate or aminophosphonate salt and a betaine-based surfactant composition of matter.
Description
“COMPOSIÇÃO AQUOSA HERBICIDA, E, PROCESSO PARA A PREPARAÇÃO DE UMA COMPOSIÇÃO’*“WATER HERBICIDE COMPOSITION, AND, PROCESS FOR THE PREPARATION OF A COMPOSITION’ *
ANTECEDENTES DA INVENÇÃOBACKGROUND OF THE INVENTION
A presente invenção refere-se a composições de herbicidas compostas de um sal de aminofosfato ou de aminofosfonato, especialmente a composições herbicidas compostas de uma quantidade relativamente elevada de um sal de aminofosfato ou de aminofosfonato e a uma composição tensoativa baseada em betaína de matéria.The present invention relates to herbicide compositions composed of an aminophosphate or aminophosphonate salt, especially herbicidal compositions composed of a relatively high amount of an aminophosphate or aminophosphonate salt and to a surfactant composition based on matter betaine.
Entre várias apresentações de composições compostas de ^0 glifosato, as composições líquidas concentradas que podem ser diluídas pelo usuário final (tipicamente um fazendeiro) são de interesse. Usualmente, quanto maior for a concentração de glifosato, melhor será, por que o usuário final pode ajustar a concentração de uso (a quantidade de ativo aplicada no campo) ajustando a diluição, e pode evitar manipular 15 muito produto (por exemplo, quanto maior for a concentração, menor será o peso).Among various presentations of compositions composed of ^ 0 glyphosate, concentrated liquid compositions that can be diluted by the end user (typically a farmer) are of interest. Usually, the higher the glyphosate concentration, the better, because the end user can adjust the use concentration (the amount of active applied in the field) by adjusting the dilution, and can avoid handling too much product (for example, the higher the concentration, the lower the weight).
As composições concentradas podem ser compostas de uma quantidade elevada de glifosato, água, e pelo menos um composto tensoativo que pode ser útil como um auxiliar de formulação (dispersão, dissolução e/ou estabilidade do glifosato em água), e/ou como um ativador biológico (por exemplo, aumentando a eficácia do sal de glifosato, por exemplo, encorajando a umidificação de uma erva daninha a ser eliminada, ou encorajando a penetração do glifosato na erva daninha). A quantidade de glifosato, a natureza do tensoativo, a quantidade do mesmo, e possíveis 25 outros ingredientes, poderão ter também um efeito nas propriedades reológicas da composição (por exemplo, a viscosidade, ou a habilidade de ser espalhada), como tal, ou diluída. As propriedades reológicas da composição como tal ou após a diluição são importantes para fins de manuseio e de aplicação.The concentrated compositions can be composed of a high amount of glyphosate, water, and at least one surfactant compound that can be useful as a formulation aid (dispersion, dissolution and / or stability of glyphosate in water), and / or as an activator biological (for example, increasing the effectiveness of the glyphosate salt, for example, encouraging the humidification of a weed to be eliminated, or encouraging the glyphosate to penetrate the weed). The amount of glyphosate, the nature of the surfactant, the amount of the surfactant, and possible 25 other ingredients, may also have an effect on the rheological properties of the composition (for example, viscosity, or the ability to spread), as such, or diluted. The rheological properties of the composition as such or after dilution are important for handling and application purposes.
Quando a concentração do glifosato é elevada, a cristalização deve ser evitada. A cristalização pode ocorrer em temperaturas diferentes, em concentrações diferentes de glifosato, ou quando diluído com água. A cristalização é caracterizada pela formação de 5 partículas sólidas pequenas compostas de glifosato. Estas partículas pequenas podem ter impacto ruim de entupimento de filtros, entupimento de orifícios, criando problemas de descarte perigosos e desnecessários para o descarte dos cristais, perda de atividade (bio-eficácia), e/ou má repartição do ativo no campo.When the concentration of glyphosate is high, crystallization should be avoided. Crystallization can occur at different temperatures, at different concentrations of glyphosate, or when diluted with water. Crystallization is characterized by the formation of 5 small solid particles composed of glyphosate. These small particles can have a bad impact of filter clogging, orifice clogging, creating dangerous and unnecessary disposal problems for the disposal of crystals, loss of activity (bio-efficiency), and / or poor distribution of the asset in the field.
^0 Composições que são compostas de glifosato e tensoativos de aminas graxas etoxiladas são conhecidas. No entanto, estes compostos, acredita-se que sejam bastante tóxicos, irritantes ou ligeiramente biodegradáveis. Existe uma necessidade para substituir estes compostos ou para reduzir a quantidade dos mesmos nas composições.^ 0 Compositions that are composed of glyphosate and surfactants of ethoxylated fatty amines are known. However, these compounds are believed to be quite toxic, irritating or slightly biodegradable. There is a need to replace these compounds or to reduce the amount of them in the compositions.
O documento WO 01/17358 (Monsanto) descreve composições que são compostas de uma quantidade elevada de sal de isopropilamina glifosato e uma mistura tensoativa composta de um tensoativo da fórmula R-CO-NR^CRyn-COOM. A mistura tensoativa é considerada como aumentando a efetividade herbicida. O tensoativo, no entanto, é M) dispendioso e existe uma necessidade por outras soluções.WO 01/17358 (Monsanto) describes compositions that are composed of a high amount of isopropylamine glyphosate salt and a surfactant mixture composed of a surfactant of the formula R-CO-NR ^ CRyn-COOM. The surfactant mixture is considered to increase herbicidal effectiveness. The surfactant, however, is M) expensive and there is a need for other solutions.
O documento WO/063589 (Rhodia) descreve composições que são compostas de 360 g/l de sal de isopropilamina glifosato (como o equivalente de ácido glifosato, 783 g/l como a concentração de sal), um tensoativo de betaína, e pelo menos um outro composto como aminas ou 25 heteroaminas opcionalmente etoxiladas.WO / 063589 (Rhodia) describes compositions that are composed of 360 g / l of isopropylamine glyphosate salt (as the glyphosate acid equivalent, 783 g / l as the salt concentration), a betaine surfactant, and at least another compound such as amines or optionally ethoxylated heteroamines.
O documento WO 01/17358 (Albright & Wilson) descreve composições compostas de 360 g/litro de sal de isopropilamina glifosato (como equivalente do ácido glifosato), tensoativos dessalinizados de alquil betaínas ou alquil amidopropil betaínas, e opcionalmente, éter carboxilatos. O documento também descreve composições compostas de 360 g/l de isopropilamina glifosato, e tensoativos de alquil betaínas ou alquil amidopropil betaínas compostas de 6 a 12% em peso de NaCl. O documento ensina que a estabilidade da composição é ligada à presença de sais 5 inorgânicos e ensina que o nível total dos referidos sais inorgânicos, de preferência, é menor do que 0,39% em peso. As composições tendo tensoativos de alquil betaínas ou alquil amidopropil betaínas dessalinizadas são ensinados como evitando a cristalização de glifosato. Todavia, a dessalinização é dispendiosa. Existe uma necessidade por composições menos fO dispendiosas e/ou composições compostas de quantidades maiores de glifosato que não precipitem.WO 01/17358 (Albright & Wilson) describes compositions composed of 360 g / liter of isopropylamine glyphosate salt (as glyphosate acid equivalent), desalted alkyl betaine surfactants or alkyl amidopropyl betaine surfactants, and optionally, carboxyl ether. The document also describes compositions composed of 360 g / l of isopropylamine glyphosate, and surfactants of alkyl betaines or alkyl amidopropyl betaines composed of 6 to 12% by weight of NaCl. The document teaches that the stability of the composition is linked to the presence of inorganic salts and teaches that the total level of said inorganic salts is preferably less than 0.39% by weight. Compositions having alkyl betaine or desalinated alkyl amidopropyl betaine surfactants are taught as preventing glyphosate crystallization. However, desalination is expensive. There is a need for less expensive compositions and / or compositions composed of larger amounts of glyphosate that do not precipitate.
BREVE SUMÁRIO DA INVENÇÃOBRIEF SUMMARY OF THE INVENTION
A invenção avalia pelo menos uma das preocupações acima.The invention addresses at least one of the concerns above.
Assim sendo, a invenção refere-se a uma composição aquosa herbicida 15 composta de:Accordingly, the invention relates to an aqueous herbicidal composition composed of:
- pelo menos 360 g por litro de um sal de anünofosfato ou de aminofosfonato, de preferência, um sal de glifosato ou de glifosinato.- at least 360 g per liter of an anphophosphate or aminophosphonate salt, preferably a glyphosate or glyphosinate salt.
- pelo menos 80 g/l, de preferência, pelo menos 100 g/l, de um sistema tensoativo composto de:- at least 80 g / l, preferably at least 100 g / l, from a surfactant system composed of:
—0 - uma composição tensoativa de betaína de matéria composta de:—0 - a betaine surfactant composition of matter composed of:
-água,-Water,
- uma betaína tendo a fórmula R1R2R2N-CH2COO', onde:- a betaine having the formula R 1 R 2 R 2 N-CH2COO ', where:
- R1 é um grupo de hidrocarbonetos linear ou ramificado, de 25 preferência um grupo alquila contendo 3 a 30 átomos de carbono, de preferência, 3 a 20 átomos de carbono,- R 1 is a straight or branched hydrocarbon group, preferably an alkyl group containing 3 to 30 carbon atoms, preferably 3 to 20 carbon atoms,
- R2, idêntico ou diferente, é um grupo alquila C1-C3, de preferência, um grupo metila, e- R 2 , identical or different, is a C1-C3 alkyl group, preferably a methyl group, and
- pelo menos 1% em peso de um sal baseado em cloreto, de preferência um sal de cloreto de potássio, e- at least 1% by weight of a chloride-based salt, preferably a potassium chloride salt, and
- opcionalmente, pelo menos um tensoativo diferente de betaína da composição tensoativa de betaína de matéria.- optionally, at least one surfactant other than betaine from the betaine surfactant composition of matter.
De acordo com outro aspecto, a invenção refere-se a um 5 processo para a preparação de uma composição aquosa herbicida.According to another aspect, the invention relates to a process for the preparation of an aqueous herbicidal composition.
De acordo com outro aspecto, a invenção refere-se ao uso da composição tensoativa de betaína de matéria em uma composição aquosa herbicida composta de pelo menos 360 g/1 de um sal de aminofosfato ou aminofosfonato, de preferência, um sal de glifosato ou glifosinato.According to another aspect, the invention relates to the use of the surfactant composition of matter betaine in an aqueous herbicidal composition composed of at least 360 g / 1 of an aminophosphate or aminophosphonate salt, preferably a glyphosate or glyphosinate salt .
fO De acordo com outro aspecto, a invenção refere-se ao uso de um sistema tensoativo composto da composição tensoativa de betaína de matéria e opcionalmente o tensoativo diferente, em uma composição aquosa herbicida composta de pelo menos 360 g/1 de um sal de aminofosfato ou aminofosfonato, de preferência, um sal de glifosato ou glifosinato.According to another aspect, the invention relates to the use of a surfactant system composed of the betaine surfactant composition of matter and optionally the different surfactant, in an aqueous herbicidal composition composed of at least 360 g / 1 of an aminophosphate salt or aminophosphonate, preferably a glyphosate or glyphosinate salt.
A invenção também se refere ao uso da composição.The invention also relates to the use of the composition.
DESCRIÇÃO DETALHADA DA INVENÇÃODETAILED DESCRIPTION OF THE INVENTION
DefiniçõesDefinitions
No relatório descritivo atual, a não ser que seja apresentado de outra forma, as quantidades de sal de aminofosfato ou de aminofosfonato, de M preferência, um sal de glifosato ou glifosinato, são expressos como equivalentes a ácido.In the current specification, unless otherwise stated, the amounts of aminophosphate or aminophosphonate salt, preferably a glyphosate or glyphosinate salt, are expressed as acid equivalents.
No relatório descritivo atual, a não ser que seja apresentado de outra forma, as quantidades de sistema tensoativo da composição tensoativa de betaína, são as quantidades totais de uma mistura ou associação 25 (quantidades Como são), ao contrário de quantidades de material ativo, quantidades de material seco (teor de sólidos), ou semelhantes.In the current specification, unless otherwise stated, the amounts of the surfactant system of the betaine surfactant composition are the total amounts of a mixture or combination 25 (quantities as they are), as opposed to quantities of active material, amounts of dry material (solids content), or the like.
No relatório descritivo atual, a não ser que seja apresentado de outra forma, as quantidades de material ativo tensoativo, para um ingrediente ou sistema tensoativo, por exemplo a composição do material de tensoativo de betaína ou o sistema tensoativo, são definidos como a quantidade de material seco do ingrediente de o sistema tensoativo, menos a quantidade total de sal do ingrediente ou sistema tensoativo.In the current specification, unless otherwise stated, the amounts of active surfactant material, for an ingredient or surfactant system, for example the composition of the betaine surfactant material or the surfactant system, are defined as the amount of dry ingredient material of the surfactant system, minus the total amount of salt of the ingredient or surfactant system.
No relatório descritivo atual, Sais baseados em cloreto refere-se a qualquer sal tendo CF, especialmente KC1 ou NaCl. As quantidades dos mesmos podem ser determinadas por meios convencionais. As quantidades, a não ser que seja apresentado de outra forma, referem-se a quantidades por peso na composição de herbicida.In the current specification, Chloride-based salts refer to any salt having CF, especially KC1 or NaCl. Their quantities can be determined by conventional means. The amounts, unless otherwise stated, refer to amounts by weight in the herbicide composition.
No relatório descritivo atual, substancialmente nenhum cátion de sódio refere-se a quantidades de cátions de sódio menores do que 1% em peso, de preferência, menores do que 0,1% em peso, de preferência, menores do que 0,01%.In the current specification, substantially no sodium cation refers to amounts of sodium cations less than 1% by weight, preferably less than 0.1% by weight, preferably less than 0.01% .
No relatório descritivo atual, um sistema tensoativo refere-se a uma associação ou misturas tensoativas que são produzidas separadamente na composição ou como uma mistura preparada antes da introdução.In the current specification, a surfactant system refers to an association or surfactant mixtures that are produced separately in the composition or as a mixture prepared before introduction.
Os tensoativos usualmente são derivados da reação compostos de vários compostos diferentes. Estes compostos diferentes têm efeito na composição herbicida. Assim sendo, é feita referência a composição tensoativas de matéria. Assim sendo, no relatório descritivo atual, uma composição tensoativa de betaína de matéria é entendido como uma mistura composta de água, um sal baseado em cloro, a molécula ativa de tensoativo de betaína, e opcionalmente, outros compostos, tais como soluções tampão de pH.Surfactants are usually derived from the reaction composed of several different compounds. These different compounds have an effect on the herbicidal composition. Therefore, reference is made to the surfactant composition of matter. Therefore, in the current specification, a betaine surfactant composition of matter is understood as a mixture composed of water, a chlorine-based salt, the active molecule of betaine surfactant, and optionally, other compounds, such as pH buffer solutions .
Os ingredientes da composição são descritos abaixo. Qualquer combinação dos mesmos pode ser implementada e definida, e/ou preparar a composição de acordo com a invenção, e/ou os usos de acordo com a invenção.The ingredients of the composition are described below. Any combination thereof can be implemented and defined, and / or prepare the composition according to the invention, and / or the uses according to the invention.
Sal de aminofosfato ou de aminofosfonatoAminophosphate or aminophosphonate salt
Os sais de aminofosfato ou de aminofosfonato são conhecidos pela pessoa versada na técnica.The aminophosphate or aminophosphonate salts are known to the person skilled in the art.
Os sais preferidos são sais de glifosato ou de glifosinato. Glifosato refere-se a N-(fosfonometil)glicina.Preferred salts are glyphosate or glyphosinate salts. Glyphosate refers to N- (phosphonomethyl) glycine.
Glifosinato refere-se a 4-[hidroxi(metil)fosfinoil]-DL5 homoalanina.Glyphosinate refers to 4- [hydroxy (methyl) phosphinoyl] -DL5 homoalanine.
Os sais incluem:Salts include:
- sais de sódio (Na);- sodium salts (Na);
- sais de potássio (K);- potassium salts (K);
- sais de amônio tendo cátions N(R)4 + onde os grupos R, fp idênticos ou diferentes, representam um átomo de hidrogênio ou um grupo de hidrocarbonetos linear ou não linear, saturado ou insaturado Ci-C6 opcionalmente substituído por um grupo hidroxila, por exemplo, sais de isopropilamina;- ammonium salts having N (R) 4 + cations where the identical or different R, fp groups represent a hydrogen atom or a linear or non-linear, saturated or unsaturated Ci-C 6 hydrocarbon group optionally substituted by a hydroxyl group , for example, isopropylamine salts;
- sais de sulfônio; os referidos sais estando presentes sozinhos ou em uma combinação.- sulfonium salts; said salts being present alone or in a combination.
Os sais de amônio que podem especialmente ser citados, incluem os sais obtidos de aminas secundárias ou primárias, tais como isopropilamina (IPA), dimetilamina, diaminas, tais como etilenodiamina ou alcanolaminas, tais como monoetanolamina (MEA).Ammonium salts that can be specially cited include salts obtained from secondary or primary amines, such as isopropylamine (IPA), dimethylamine, diamines, such as ethylenediamine or alkanolamines, such as monoethanolamine (MEA).
ZD Trimetil sulfônio é um sal de sulfônio perfeitamente adequado.ZD Trimethyl sulfonium is a perfectly suitable sulfonium salt.
Sais de glifosato preferidos para a aplicação herbicida que podem ser citados são o sal de isopropilamina (IPA), o sal de monoetanolamina (MEA), sal de trimetilsulfônio, sal de potássio, sal de amônio, e misturas ou associações dos mesmos, por exemplo, conforme 25 ensinado nos documentos WO 01/26469 (Nufarm) e WO 03/013241 (Nufarm).Preferred glyphosate salts for herbicidal application that can be cited are the isopropylamine salt (IPA), the monoethanolamine salt (MEA), trimethylsulfonium salt, potassium salt, ammonium salt, and mixtures or combinations thereof, for example , as taught in WO 01/26469 (Nufarm) and WO 03/013241 (Nufarm).
Na presente invenção, são preferidos sais contendo isopropilamina. Assim sendo, em uma realização preferida, o sal é um sal de isopropilamina glifosato. Em uma realização preferida, a relação entre o cátion, como o cátion de isopropilamina e glifosato é em tomo de 1/1. No entanto, a relação pode ser maior do que 1/1. Tal relação produz composições tendo um pH maior. Quanto maior for o pH, menor será a cristalização. O pH pode também ser controlado utilizando-se qualquer composto básico, como 5 por exemplo, KOH ou outras soluções tampão.In the present invention, isopropylamine-containing salts are preferred. Accordingly, in a preferred embodiment, the salt is an isopropylamine glyphosate salt. In a preferred embodiment, the relationship between the cation, such as the isopropylamine cation and glyphosate, is about 1/1. However, the ratio can be greater than 1/1. Such a relationship produces compositions having a higher pH. The higher the pH, the lower the crystallization. The pH can also be controlled using any basic compound, such as 5 for example, KOH or other buffer solutions.
Sistema tensoativoSurfactant system
O sistema tensoativo é composto da composição tensoativa de betaína de matéria e opcionalmente pelo menos um tensoativo diferente da betaína da composição tensoativa de betaína de matéria. Tensoativos fO diferentes podem ser fornecidos na composição herbicida como um ingrediente separado; eles podem portanto ser referidos como uma associação. Em outra realização, pelo menos um tensoativo diferentes pode ser fornecido como uma mistura com a composição tensoativa de betaína de matéria, ele podendo portanto ser referido como uma mistura. Naquela realização, o 15 tensoativo diferente pode ser preparados separadamente ou simplesmente misturado com a composição tensoativa de betaína de matéria, ou preparado pelo mesmo processo de preparação da composição tensoativa de betaína de matéria. Alguns tensoativos diferentes úteis são descritos abaixo como ingredientes adicionais e como tensoativos adicionais.The surfactant system is composed of the betaine surfactant composition of matter and optionally at least one surfactant other than the betaine of the betaine surfactant composition of matter. Different fO surfactants can be provided in the herbicidal composition as a separate ingredient; they can therefore be referred to as an association. In another embodiment, at least one different surfactant can be supplied as a mixture with the betaine surfactant composition of matter, it can therefore be referred to as a mixture. In that embodiment, the different surfactant can be prepared separately or simply mixed with the matter betaine surfactant composition, or prepared by the same process of preparing the matter betaine surfactant composition. Some different useful surfactants are described below as additional ingredients and as additional surfactants.
Composição tensoativa de betaína de matéria:Betaine surfactant composition of matter:
Os tensoativos usualmente são derivados da reação compostos de vários compostos diferentes. Estes compostos diferentes têm efeito na composição herbicida. Assim sendo eles são referidos como uma composição tensoativa de matéria.Surfactants are usually derived from the reaction composed of several different compounds. These different compounds have an effect on the herbicidal composition. So they are referred to as a surfactant composition of matter.
A composição tensoativa de betaína de matéria é composta de:The betaine surfactant composition of matter is composed of:
-água,-Water,
- uma betaína tendo a fórmula R1R2R2N'-CH2COO·, onde:- a betaine having the formula R 1 R 2 R 2 N'-CH 2 COO ·, where:
- R1 é um grupo de hidrocarbonetos linear ou ramificado, de preferência, um grupo alquila contendo 3 a 30 átomos de carbono, de preferência, 3 a 20 átomos de carbono,- R 1 is a straight or branched hydrocarbon group, preferably an alkyl group containing 3 to 30 carbon atoms, preferably 3 to 20 carbon atoms,
- R2, idêntico ou diferente, é um grupo alquila CrC3, de preferência, um grupo metila,- R 2 , identical or different, is a C r C 3 alkyl group, preferably a methyl group,
- pelo menos 1% em peso de um sal baseado em cloreto, de 5 preferência, um sal de cloreto de potássio.- at least 1% by weight of a chloride-based salt, preferably a potassium chloride salt.
A betaína é um composto principal do tensoativo da composição tensoativa de betaína de matéria. Ela, de preferência, é um composto tensoativo principal do sistema tensoativo. Ela também é referida como o tensoativo principal. Composto tensoativo principal significa que o ^0 referido composto tensoativo representa o tensoativo mais elevado importante comparado com outros tensoativos opcionais. Por exemplo, em uma mistura ou associação composta de 40 partes de ativo do tensoativo 1, 30 partes como o ativo do tensoativo 2, e 30 partes como o ativo do tensoativo 3, o tensoativo 1 seria considerado como o tensoativo principal, mesmo se ele representa 15 menos de 50% de todos os tensoativos.Betaine is a major surfactant compound of the betaine surfactant composition of matter. It is preferably a major surfactant in the surfactant system. It is also referred to as the main surfactant. Main surfactant compound means that the said 0 surfactant compound represents the highest important surfactant compared to other optional surfactants. For example, in a mixture or combination consisting of 40 parts of surfactant 1, 30 parts as surfactant 2, and 30 parts as surfactant 3, surfactant 1 would be considered as the main surfactant, even if it represents 15 less than 50% of all surfactants.
De preferência, o ativo principal de betaína representa pelo menos 30% em peso, de preferência pelo menos 50%, do ativo principal de total de tensoativo do sistema tensoativo na composição.Preferably, the main betaine asset represents at least 30% by weight, preferably at least 50%, of the total surfactant main asset of the surfactant system in the composition.
Vantajosamente, a composição tensoativa de betaína de M) matéria é composta de:Advantageously, the betaine surfactant composition of M) matter is composed of:
-água,-Water,
- pelo menos 25%, de preferência, pelo menos 30% em peso como o tensoativo ativo principal da betaína,- at least 25%, preferably at least 30% by weight, as the main active surfactant in betaine,
- pelo menos 2%, de preferência, pelo menos 5% em peso de 25 um sal de cloreto de potássio.- at least 2%, preferably at least 5% by weight of a potassium chloride salt.
De preferência, a composição tensoativa de betaína de matéria é composta de:Preferably, the betaine surfactant composition of matter is composed of:
- água,- Water,
- pelo menos 30%, de preferência, pelo menos 35% em peso do tensoativo ativo principal de betaína,- at least 30%, preferably at least 35% by weight of the main active betaine surfactant,
- pelo menos 5% em peso de um sal de cloreto de potássio, e- at least 5% by weight of a potassium chloride salt, and
- substancialmente nenhum cátion de sódio.- substantially no sodium cation.
Em uma realização preferida, a quantidade total de sais inorgânicos no sistema tensoativo, de preferência, de sais com base em cloreto, é maior do que 0,4% em peso, e de preferência, é maior do que 1% em peso.In a preferred embodiment, the total amount of inorganic salts in the surfactant system, preferably chloride-based salts, is greater than 0.4% by weight, and preferably, greater than 1% by weight.
Em uma realização preferida, a quantidade de sais inorgânicos, de preferência, de sais com base em cloreto, é maior do que 8%, de preferência, maior do que 10%, de preferência, maior do que 12%, em peso da quantidade de composição tensoativa de betaína de matéria.In a preferred embodiment, the amount of inorganic salts, preferably chloride-based salts, is greater than 8%, preferably greater than 10%, preferably greater than 12%, by weight of the amount of betaine surfactant composition of matter.
Em uma realização preferida, a quantidade total de sais inorgânicos, de preferência de sais com base em cloreto, é maior do que 8%, de preferência, maior do que 10%, de preferência, maior do que 12% em peso da quantidade de sistema tensoativo.In a preferred embodiment, the total amount of inorganic salts, preferably chloride-based salts, is greater than 8%, preferably greater than 10%, preferably greater than 12% by weight of the amount of surfactant system.
A betaína, de preferência tem R2 como sendo um grupo metila (alquildimetilbetaína).Betaine preferably has R 2 as a methyl group (alkyldimethylbetaine).
R1 é um grupo alquila. Este grupo usualmente é na realidade uma mistura de grupos diferentes tendo quantidades diferentes de átomos de carbono, sendo lineares ou ramificados, e opcionalmente, tendo algumas insaturações. Estas misturas são provenientes de reagentes usados para prepará-las, que na realidade são cortes de destilação e/ou têm uma origem natural. No relatório descritivo atual, a quantidade de átomos de carbono no grupo R1 refere-se ao número de átomos de carbono das duas espécies mais representadas.R 1 is an alkyl group. This group is usually actually a mixture of different groups having different amounts of carbon atoms, being linear or branched, and optionally, having some unsaturation. These mixtures come from reagents used to prepare them, which are actually distillation cuts and / or have a natural origin. In the current specification, the amount of carbon atoms in the R 1 group refers to the number of carbon atoms of the two most represented species.
Em uma realização preferida:In a preferred embodiment:
- R2 é um grupo metila, e- R 2 is a methyl group, and
- R1 é uma mistura do grupo lauril alquila, tendo mais de 50% em peso de C12.- R 1 is a mixture of the lauryl alkyl group, having more than 50% by weight of C12.
A composição tensoativa de betaína de matéria pode ser obtida, e de preferência é obtida, de um processo que é composto das seguintes etapas:The betaine surfactant composition of matter can be obtained, and preferably is obtained, from a process that is composed of the following steps:
Etapa 1) a reação de um composto da fórmula RJJVJVN com 5 ácido cloroacético, para obter um produto da reação;Step 1) the reaction of a compound of the formula RJJVJVN with 5 chloroacetic acid, to obtain a reaction product;
Etapa 2) adição de hidróxido de potássio para aumentar o pH,Step 2) adding potassium hydroxide to increase the pH,
Etapa 3) opcionalmente, a adição de alguns ingredientes adicionais ou ajuste da concentração e do pH.Step 3) optionally, adding some additional ingredients or adjusting the concentration and pH.
É mencionado que a etapa 1 e a etapa 2 também podem ser f0 executadas simultaneamente, pela adição de hidróxido de potássio durante o término da reação ou pela adição progressiva de ácido cloro-acético e hidróxido de potássio.It is mentioned that step 1 and step 2 can also be carried out simultaneously, by the addition of potassium hydroxide during the termination of the reaction or by the progressive addition of chlor-acetic acid and potassium hydroxide.
Em outra realização, o cloro acetato de potássio é utilizado na etapa 1) ao invés do ácido cloro-acético, e a etapa 2) é opcional.In another embodiment, chlorine potassium acetate is used in step 1) instead of chlor-acetic acid, and step 2) is optional.
Em uma realização preferida, o processo não inclui nenhuma etapa de dessalinização ou etapa de troca de íons. Assim sendo, o processo é efetivo em custo, e portanto a composição herbicida também pode ser interessante do ponto de vista de custo.In a preferred embodiment, the process does not include any desalination or ion exchange steps. Therefore, the process is cost effective, and therefore the herbicidal composition can also be interesting from a cost perspective.
Vantajosamente, o pH da composição tensoativa de betaína de matéria é de 6 a 8, em uma solução de água a 1% em peso.Advantageously, the pH of the betaine surfactant composition of matter is 6 to 8, in a 1% by weight water solution.
Outros ingredientesOther ingredients
A composição herbicida pode ser composta de outros ingredientes, tais como:The herbicidal composition can be composed of other ingredients, such as:
- tensoativos diferentes de betaína da composição tensoativa de betaína de matéria, como parte do sistema tensoativo,- surfactants other than betaine from the betaine surfactant composition of matter, as part of the surfactant system,
- agentes anti-espumantes,- defoaming agents,
- solventes, de preferência, solventes miscíveis em água, de preferência, solventes polares, ou- solvents, preferably water-miscible solvents, preferably polar solvents, or
- agentes de controle de deposição, tais como agentes anti- rebote, ou anti-flutuante, opcionalmente adicionados posteriormente.- deposition control agents, such as anti-rebound, or anti-floating agents, optionally added later.
A pessoa versada na técnica conhece outros ingredientes que podem ser utilizados para o controle de algumas propriedades ou características da composição e/ou para a adição de benefícios.The person skilled in the art knows other ingredients that can be used to control some properties or characteristics of the composition and / or to add benefits.
As formulações podem, por exemplo, ser compostas de:Formulations can, for example, be composed of:
- agente anti-espumante organopolisiloxano;- organopolysiloxane defoaming agent;
- agentes de espessamento, tais como polissacarídeos do tipo de goma de xantano, alginatos, metil celuloses carboxiladas ou etoxiladas, macromoléculas sintéticas do tipo de poliacrilato, polimaleato, fO polivinilpirrolidona, polietileno glicol e álcool polivinílico, ou do tipo inorgânico como bentonitas.- thickening agents, such as xanthan gum type polysaccharides, alginates, carboxylated or ethoxylated methyl celluloses, synthetic macromolecules of the polyacrylate type, polymaleate, polyvinylpyrrolidone, polyethylene glycol and polyvinyl alcohol, or inorganic type such as bentonites.
- aditivos auxiliares tais como antioxidantes, agentes anti-UV, corantes, etc.- auxiliary additives such as antioxidants, anti-UV agents, dyes, etc.
- solventes, tais como álcool, por exemplo, isopropanol, 15 tipicamente até 15% em peso.- solvents, such as alcohol, for example, isopropanol, typically up to 15% by weight.
A quantidade destes aditivos listada acima normalmente é menor do que 10% em peso, de preferência, 1% em peso ou menos, vantajosamente, 0,1% em peso ou menos, comparado com o peso da composição.The amount of these additives listed above is usually less than 10% by weight, preferably 1% by weight or less, advantageously 0.1% by weight or less, compared to the weight of the composition.
ZD Outros tensoativosZD Other surfactants
A composição herbicida pode ser composta de um tensoativo adicional, diferente da betaína da composição tensoativa de betaína de matéria. Este tensoativo adicional pode produzir outras vantagens ou sinergias em termos de custo, e/ou bio-eficácia, e/ou controle da reologia, e/ou 25 preocupações ambientais e/ou preocupações de sensibilidade.The herbicidal composition can be composed of an additional surfactant, different from the betaine of the betaine surfactant composition of matter. This additional surfactant may produce other advantages or synergies in terms of cost, and / or bio-efficacy, and / or control of rheology, and / or environmental concerns and / or sensitivity concerns.
Exemplos de outros tensoativos incluem:Examples of other surfactants include:
- uma amina graxas etoxilada, uma amina graxa,- an ethoxylated fatty amine, a grease amine,
- um éter carboxilato,- a carboxyl ether,
- um mono- e di-éster fosfato ácido ou não ácido, opcionalmente polialcoxilado,- an acidic or non-acidic phosphate mono- and di-ester, optionally polyalkoxylated,
- um alquil monoglicosídeo ou alquil poliglicosídeo, vantajosamente octil glicosídeo, octil poliglicosídeo, decil glicosídeo, decil poliglicosídeo, ou uma mistura dos mesmos, ou- an alkyl monoglycoside or alkyl polyglycoside, advantageously octyl glycoside, octyl polyglycoside, decyl glycoside, decyl polyglycoside, or a mixture thereof, or
- misturas dos mesmos.- mixtures thereof.
As aminas graxas ou aminas graxas etoxiladas podem ser compostas de pelo menos um grupo de hidrocarbonetos contendo 2 a 24 átomos de carbono, opcionalmente poli-alcoxilados.Fatty amines or ethoxylated fatty amines can be composed of at least one hydrocarbon group containing 2 to 24 carbon atoms, optionally poly-alkoxylated.
As aminas graxas ou aminas graxas etoxiladas podem ser mais fp especialmente escolhidas de aminas que são compostas pelo menos de um grupo linear ou ramificado, saturado ou insaturado, contendo 2 a 24 átomos de carbono, de preferência, 8 a 18 átomos de carbono, opcionalmente, sendo compostos de 2 a 30 grupos de óxido de etileno, ou uma mistura de uma quantidade dos mesmos. Exemplos incluem aminas de sebo etoxiladas.The fatty amines or ethoxylated fatty amines can be more specially chosen from amines that are composed of at least one linear or branched, saturated or unsaturated group, containing 2 to 24 carbon atoms, preferably 8 to 18 carbon atoms, optionally , being composed of 2 to 30 ethylene oxide groups, or a mixture of an amount thereof. Examples include ethoxylated tallow amines.
As aminas graxas ou aminas graxas etoxiladas podem ser escolhidas de aminas graxas etoxiladas compostas pelo menos de um grupo linear ou ramificado, saturado ou insaturado contendo 6 a 24 átomos de carbono, de preferência, 8 a 20 átomos de carbono, compostos de 2 a 30 grupos de óxido de etileno, ou uma mistura de uma quantidade dos mesmos.Fatty amines or ethoxylated fatty amines can be chosen from ethoxylated fatty amines composed of at least one linear or branched, saturated or unsaturated group containing 6 to 24 carbon atoms, preferably 8 to 20 carbon atoms, compounds from 2 to 30 ethylene oxide groups, or a mixture of an amount thereof.
Ξ3 Exemplos incluem os compostos tendo a seguinte fórmula:Ξ3 Examples include compounds having the following formula:
(OAJn /(OAJn /
R-O-(CH2)3-N \RO- (CH 2 ) 3 -N \
(OA)h· onde R representa um grupo de hidrocarbonetos linear ou ramificado, saturado ou insaturado, contendo 6 a 24 átomos de carbono, de preferência, 8 a 20 átomos de carbono; OA representa um grupo oxipropileno; e n, ri, que poderá ou não ser idêntico, representa um número 25 médio na faixa de 1 a 30.(OA) h · where R represents a straight or branched, saturated or unsaturated hydrocarbon group, containing 6 to 24 carbon atoms, preferably 8 to 20 carbon atoms; OA represents an oxypropylene group; en, ri, which may or may not be identical, represents an average number 25 in the range 1 to 30.
Exemplos de tais aminas podem ser citados como aminas derivadas de copra e contendo 5 grupos oxietileno (OE), oleico-aminas contendo 5 OE, aminas derivadas de sebo contendo 5 - 20 OE, por exemplo, compostos correspondendo à fórmula acima, nos quais R é um grupo alquila contendo 12 a 15 átomos de carbono, o número de grupos OE estando na faixa de 20 a 30.Examples of such amines can be cited as amines derived from copra and containing 5 oxyethylene (OE) groups, oleic amines containing 5 OE, tallow amines containing 5 - 20 OE, for example, compounds corresponding to the above formula, in which R is an alkyl group containing 12 to 15 carbon atoms, the number of OE groups being in the range of 20 to 30.
A quantidade de aminas graxas ou aminas graxas etoxiladas pode ser de 0 (nenhum) a 120 g/1 da composição, de preferência, de 0 (nenhum) a 60 g/1.The amount of fatty amines or ethoxylated fatty amines can be from 0 (none) to 120 g / 1 of the composition, preferably from 0 (none) to 60 g / 1.
O éter carboxilato, de preferência, tem a fórmula R(0CH2CH2)nOCH2C02; onde R é um grupo linear ou ramificado alquila, alquenila, alquilfenila ou polipropileno-oxila tendo 6 a 20, por exemplo, S a 1 átomos de carbono alifáticos e n é 1 a 30, de preferência, 2 a 20. O éter carboxilato, de preferência, tem um contra-íon de amônio ou potássio, ou obtido de uma amina ou alcanolamina tendo até 6 átomos de carbono.The carboxylate ether preferably has the formula R (0CH 2 CH2) nOCH 2 CO2; where R is a linear or branched alkyl, alkenyl, alkylphenyl or polypropylene oxyl group having 6 to 20, for example, S to 1 aliphatic carbon atoms and n is 1 to 30, preferably 2 to 20. Carboxylate ether, of preferably, it has an ammonium or potassium counterion, or obtained from an amine or alkanolamine having up to 6 carbon atoms.
O mono- e di-éster fosfato ácido ou não ácido, opcionalmente poli-alcoxilado é escolhido de mono- ou di-ésteres fosfatos ácidos ou não ácidos, opcionalmente poli-alcoxilados, com a fórmula abaixo:The acid or non-acid phosphate mono- and di-ester, optionally poly-alkoxylated is chosen from acid or non-acid phosphate mono- or di-esters, optionally poly-alkoxylated, with the formula below:
(AO)3.mP(=O)(OM)m onde:(AO) 3 . m P (= O) (OM) m where:
- A, idêntico ou diferente, representa um grupo Rn-O(CH2CHR’2-O)n onde:- A, identical or different, represents a group R n -O (CH2CHR ' 2 -O) n where:
- R'1, idêntico ou diferente, representa um grupo de hidrocarbonetos C6-C2o saturado ou insaturado, linear ou não linear, de preferência, Cg-Cig;- R ' 1 , identical or different, represents a group of C 6 -C 2 saturated or unsaturated hydrocarbons, linear or non-linear, preferably Cg-Cig;
- R'2, idêntico ou diferente, representa um átomo de hidrogênio ou um grupo metila ou etila, de preferência, um átomo de hidrogênio;- R ' 2 , identical or different, represents a hydrogen atom or a methyl or ethyl group, preferably a hydrogen atom;
- n é um número médio de grupos na faixa de 0 a 10, de preferência, na faixa de 2 a 10;- n is an average number of groups in the range 0 to 10, preferably in the range 2 to 10;
- M, idêntico ou diferente, representa um átomo de hidrogênio, um metal alcalino ou alcalino terroso, um radical do tipo N(R3)4 + onde R3, idêntico ou diferente, representa um átomo de hidrogênio ou um grupo de hidrocarbonetos Ci-Ce saturado ou insaturado, linear ou não linear, opcionalmente substituído com um grupo hidroxila;- M, identical or different, represents a hydrogen atom, an alkali or alkaline earth metal, a radical of type N (R 3 ) 4 + where R 3 , identical or different, represents a hydrogen atom or a group of Ci hydrocarbons -Ce saturated or unsaturated, linear or non-linear, optionally substituted with a hydroxyl group;
- m é um número inteiro ou médio na faixa de 1 a 2.- m is an integer or average number in the range 1 to 2.
O mono- ou di-éster fosfato ácido ou não ácido, opcionalmente poli-alcoxilado pode estar na forma de um mono-éster, um di-éster, ou uma mistura destes dois ésteres.The acidic or non-acidic, optionally poly-alkoxylated mono- or di-ester phosphate can be in the form of a mono-ester, a di-ester, or a mixture of these two esters.
A quantidade de mono- e di-éster fosfato ácido ou não ácido, opcionalmente polialcoxilado pode ser de 0 (nenhum) a 120 g/l da composição.The amount of acid or non-acid phosphate mono- and di-ester, optionally polyalkoxylated, can be from 0 (none) to 120 g / l of the composition.
Processo para a preparação da composição herbicida.Process for the preparation of the herbicidal composition.
As composições da invenção podem ser preparadas misturando-se os seus constituintes diferentes com agitação moderada.The compositions of the invention can be prepared by mixing their different constituents with moderate agitation.
Esta operação, de preferência, acontece em uma temperatura na faixa de 15 °C a 60 °C, de preferência, em uma temperatura próxima da temperatura ambiente (15 - 30 °C).This operation preferably takes place at a temperature in the range of 15 ° C to 60 ° C, preferably at a temperature close to the ambient temperature (15 - 30 ° C).
Μ) A composição tensoativa de matéria de preferência é adicionada tão logo os outros constituintes foram misturados.Μ) The surfactant composition of matter is preferably added as soon as the other constituents have been mixed.
Assim sendo, um processo preferido completo pode ser composto das seguintes etapas:Therefore, a complete preferred process can consist of the following steps:
- etapa a) preparação de uma composição tensoativa de matéria 25 através de um processo que é composto das seguintes etapas:- step a) preparation of a surfactant composition of matter 25 through a process that consists of the following steps:
etapa 1) reação de um composto da fórmula R!R2R2N com ácido cloro-acético para obter-se um produto da reação;step 1) reaction of a compound of the formula R ! R 2 R 2 N with chloro-acetic acid to obtain a reaction product;
etapa 2) adição de hidróxido de potássio para aumentar o pH, etapa 3) opcionalmente, a adição de alguns ingredientes adicionais ou ajuste da concentração ou do pH.step 2) adding potassium hydroxide to increase the pH, step 3) optionally adding some additional ingredients or adjusting the concentration or pH.
- etapa b) mistura do sal de aminofosfato ou aminofosfonato, a composição tensoativa de matéria e opcionalmente outros ingredientes.- step b) mixing the aminophosphate or aminophosphonate salt, the surfactant composition of matter and optionally other ingredients
A etapa b), por exemplo, é composta das etapas de produção de uma mistura de água e do sal de aminofosfato ou de aminofosfonato, e então a adição da composição tensoativa de matéria.Step b), for example, is composed of the steps of producing a mixture of water and the aminophosphate or aminophosphonate salt, and then adding the surfactant composition of matter.
É mencionado que a etapa 1 e a etapa 2 também podem ser executadas simultaneamente, pela adição de hidróxido de potássio durante o término da reação ou pela adição progressiva de ácido cloro-acético e hidróxido de potássio.It is mentioned that step 1 and step 2 can also be carried out simultaneously, by the addition of potassium hydroxide during the completion of the reaction or by the progressive addition of chloro-acetic acid and potassium hydroxide.
Em outra realização, cloro-acetato de potássio é utilizado na etapa 1) ao invés de ácido cloro-acético, e a etapa 2) é opcional.In another embodiment, potassium chloro-acetate is used in step 1) instead of chlor-acetic acid, and step 2) is optional.
Características preferidas da composição herbicidaPreferred characteristics of the herbicidal composition
Vantajosamente, na composição herbicida, a quantidade total de material ativo tensoativo é pelo menos de 24 g/l.Advantageously, in the herbicidal composition, the total amount of active surfactant material is at least 24 g / l.
Vantajosamente, o material ativo tensoativo é pelo menos 25% em peso do sistema tensoativo. Em outras palavras, o sistema tensoativo tem pelo menos 25% em peso como material ativo tensoativo de betaína juntamente com tensoativos diferentes opcionais.Advantageously, the active surfactant material is at least 25% by weight of the surfactant system. In other words, the surfactant system has at least 25% by weight as a betaine surfactant active material together with optional different surfactants.
Vantajosamente, a composição de herbicida é composta pelo menos de 80 g/l, de preferência, pelo menos 100 g/l, da composição tensoativa de betaína de matéria. Assim sendo, a composição tensoativa de betaína de matéria representa o todo de uma parte do sistema tensoativo na composição herbicida.Advantageously, the herbicide composition is composed of at least 80 g / l, preferably at least 100 g / l, of the betaine surfactant composition of matter. Therefore, the betaine surfactant composition of matter represents the whole of a part of the surfactant system in the herbicidal composition.
Vantajosamente, a composição herbicida é composta de:Advantageously, the herbicidal composition is composed of:
- de 360 g/l a 560 g/l do sal de aminofosfato ou de aminofosfonato, de preferência, de sal de glifosato, de preferência, de sal de isopropilamina glifosato, e- from 360 g / l to 560 g / l of the aminophosphate or aminophosphonate salt, preferably the glyphosate salt, preferably the isopropylamine glyphosate salt, and
- de 80 g/l a 160 g/l do sistema tensoativo, de preferência, da composição tensoativa de betaína de matéria.- from 80 g / l to 160 g / l of the surfactant system, preferably of the betaine surfactant composition of matter.
Vantajosamente, a composição é composta de:Advantageously, the composition is composed of:
- de 400 a 500 g/litro de sal de glifosato, de preferência, de sal de isopropilamina glifosato, e- 400 to 500 g / liter of glyphosate salt, preferably isopropylamine glyphosate salt, and
- de 100 a 135 g/1 do sistema tensoativo, de preferência, da composição tensoativa de betaína de matéria.- from 100 to 135 g / 1 of the surfactant system, preferably of the betaine surfactant composition of matter.
De preferência, a composição é composta de:Preferably, the composition is composed of:
- pelo menos 500 g/1 do sal de glifosato, de preferência, do sal de isopropilamina glifosato, e- at least 500 g / 1 of the glyphosate salt, preferably the isopropylamine glyphosate salt, and
- pelo menos 120 g/1, de preferência pelo menos 135 g/1, do sistema tensoativo, de preferência, da composição tensoativa de betaína de matéria.- at least 120 g / 1, preferably at least 135 g / 1, of the surfactant system, preferably of the betaine surfactant composition of matter.
É preferível que a quantidade total de sais inorgânicos na composição, de preferência, de sais com base em cloreto, seja maior do que 15 0,4% em peso, e de preferência, maior do que 1% em peso.It is preferred that the total amount of inorganic salts in the composition, preferably chloride-based salts, be greater than 15 0.4% by weight, and preferably greater than 1% by weight.
Em cargas elevadas de sal de glifosato, especialmente com sais diferentes de sais de potássio, por exemplo, com sal de isopropilamina glifosato, a invenção permite entre outros a manipulação de menos composição (carga menor), com uma boa estabilidade (nenhum cristal) com M) uma bio-eficácia e/ou perfil tóxico interessante.At high loads of glyphosate salt, especially with salts other than potassium salts, for example, with isopropylamine glyphosate salt, the invention allows, among others, the handling of less composition (lower load), with good stability (no crystal) with M) an interesting bio-efficacy and / or toxic profile.
Em baixas cargas de sal de glifosato, e especialmente com sais diferentes de sais de potássio, por exemplo, com sal de isopropilamina glifosato, a invenção permite entre outros uma boa estabilidade (nenhum cristal) com uma bio-eficácia e/ou perfil tóxico interessante e assim a carga de 25 tensoativo pode ser aumentada.At low loads of glyphosate salt, and especially with salts other than potassium salts, for example, with isopropylamine glyphosate salt, the invention allows, among others, good stability (no crystal) with a bio-efficacy and / or interesting toxic profile and so the surfactant load can be increased.
Utilização a jusanteDownstream use
A composição de herbicida da invenção pode portanto ser utilizada para tratar plantas, normalmente após a diluição com água. A composição diluída pode ser aplicada sobre um campo por qualquer meioThe herbicide composition of the invention can therefore be used to treat plants, usually after dilution with water. The diluted composition can be applied to a field by any means
apropriado.appropriate.
A diluição, e a aplicação sobre o campo, pode por exemplo, ser tal que a quantidade de sal de aminofosfato ou de aminofosfonato, de preferência, sal de glifosato, seja de 500 g de equivalente de ácido/ha a 1.500 5 g de equivalente de ácido/ha, tipicamente, de 600 a 1.200 g/ha.The dilution, and the application on the field, can for example be such that the amount of aminophosphate or aminophosphonate salt, preferably glyphosate salt, is 500 g of acid equivalent / ha to 1,500 5 g of equivalent acid / ha, typically 600 to 1,200 g / ha.
Após a diluição o usuário final pode misturar outros herbicidas, pesticidas, fertilizantes, fungicidas. Por exemplo, o usuário final pode combinar o sal de glifosato com outros herbicidas para equacionar algumas resistências de ervas daninhas ao glifosato. A ]0 composição de acordo com a invenção, especialmente com sal de glifosato diferente de sal de potássio, por exemplo, com sal de isopropilamina glifosato, produz uma boa compatibilidade com outros herbicidas. A invenção pode permitir cargas elevadas de sais de glifosato com boa compatibilidade.After dilution the end user can mix other herbicides, pesticides, fertilizers, fungicides. For example, the end user can combine the glyphosate salt with other herbicides to equate some weed resistance to glyphosate. A] The composition according to the invention, especially with glyphosate salt other than potassium salt, for example, with isopropylamine glyphosate salt, produces good compatibility with other herbicides. The invention can allow high loads of glyphosate salts with good compatibility.
Alguns detalhes ou vantagens da invenção aparecerão nos exemplos não limitativos abaixo.Some details or advantages of the invention will appear in the non-limiting examples below.
EXEMPLOSEXAMPLES
Os seguintes ingredientes são utilizados:The following ingredients are used:
Tensoativo 1: composição tensoativa de matéria composta dos seguintes: -0 - alquildimetilbetaína, onde a alquila é uma mistura de cerca de 70% em peso de laurila (C12) e cerca de 30% em peso de tetradecila (Cu),Surfactant 1: surfactant composition of matter composed of the following: -0 - alkyldimethylbetaine, where alkyl is a mixture of about 70% by weight of lauryl (C 12 ) and about 30% by weight of tetradecyl (Cu),
- sólidos: cerca de 41% em peso- solids: about 41% by weight
- KC1: cerca de 9% em peso- KC1: about 9% by weight
Tensoativo 2: Mirataine D40, comercializada pela RhodiaSurfactant 2: Mirataine D40, marketed by Rhodia
Tensoativo 3: Terwet 3780 etoxilato de amina de sebo, Hunstman Glifosato: sal de isopropilamina glifosato (46% de equivalente de ácido por peso)Surfactant 3: Terwet 3780 tallow amine ethoxylate, Hunstman Glyphosate: isopropylamine glyphosate salt (46% acid equivalent by weight)
As seguintes composições são preparadas (C representa comparativo, e ae representa equivalente ácido). Tabela:The following compositions are prepared (C represents comparative, and e represents acid equivalent). Table:
O estudo mostra que a composição de acordo com a invenção tem uma estabilidade boa surpreendente, sem a formação de cristais.The study shows that the composition according to the invention has surprisingly good stability, without the formation of crystals.
No meio tempo, as composições de acordo com os exemplos têm uma bio-eficácia melhor (menor peso fresco) e/ou mais rápida (escurecimento maior) em pelo menos algumas ervas daninhas significativas (azevém anual e rabanete selvagem).In the meantime, the compositions according to the examples have better bio-efficacy (less fresh weight) and / or faster (greater browning) in at least some significant weeds (annual ryegrass and wild radish).
Claims (10)
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| US60/640,300 | 2004-12-30 | ||
| PCT/EP2005/014131 WO2006069791A1 (en) | 2004-12-30 | 2005-12-30 | Herbicidal composition comprising an aminophosphate or aminophosphonate salt and a betaine |
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Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2005321478B2 (en) * | 2004-12-30 | 2009-11-05 | Specialty Operations France | Herbicidal composition comprising an aminophosphate or aminophosphonate salt and a betaine |
| NZ567994A (en) * | 2005-11-14 | 2012-03-30 | Rhodia | Surfactant is sodium alkyl ether sulfate in agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions |
| WO2008066611A2 (en) | 2006-10-16 | 2008-06-05 | Rhodia Inc. | Agricultural adjuvant compositions. pesticide compositions. and methods for using such compositions |
| FR2913350B1 (en) * | 2007-03-08 | 2010-05-21 | Rhodia Recherches & Tech | USE OF BETAINE AS FOAMING AGENT AND FOAM DRAIN REDUCTION AGENT |
| FR2914647B1 (en) * | 2007-04-05 | 2011-10-21 | Rhodia Recherches Et Tech | COPOLYMER COMPRISING BETAINIC UNITS AND HYDROPHOBIC AND / OR AMPHIPHILIC UNITS, PREPARATION METHOD, AND USES. |
| CN101932236A (en) * | 2007-11-07 | 2010-12-29 | 罗地亚管理公司 | Herbicidal composition comprising an aminophosphate or aminophosphonate salt and a viscosity-reducing agent |
| HRP20160477T1 (en) * | 2008-06-18 | 2016-06-17 | Stepan Company | Ultra-high loading glyphosate concentrate |
| WO2010002836A2 (en) | 2008-07-03 | 2010-01-07 | Mosanto Technology Llc | Combinations of derivatized saccharide surfactants and etheramine oxide surfactants as herbicide adjuvants |
| US8748344B2 (en) | 2009-07-14 | 2014-06-10 | Rhodia Operations | Agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions |
| US9137988B2 (en) * | 2009-09-02 | 2015-09-22 | Akzo Nobel Chemicals International B.V. | Nitrogen containing surfactants for agricultural use |
| US8841235B2 (en) | 2010-08-10 | 2014-09-23 | Rhodia Operations | Agricultural pesticide compositions |
| EP2632271B1 (en) | 2010-10-25 | 2018-12-05 | Stepan Company | Glyphosate formulations based on compositions derived from natural oil metathesis |
| EP2505061A1 (en) | 2011-03-30 | 2012-10-03 | Rhodia Opérations | New uses of choline chloride in agrochemical formulations |
| CA2889198C (en) | 2012-10-23 | 2023-02-21 | Rhodia Operations | Aqueous pesticide compositions comprising a fatty deposition control agent |
| BR102012028537B1 (en) | 2012-11-07 | 2018-10-23 | Oxiteno S/a Industria E Comércio | surfactant composition, glyphosate containing herbicidal formulation, and use of the glyphosate containing herbicidal formulation |
| CA3006787A1 (en) * | 2015-12-09 | 2017-06-15 | Akzo Nobel Chemicals International B.V. | Low foaming high electrolyte compositions |
| EP3478256A4 (en) * | 2016-06-30 | 2020-02-26 | Rhodia Operations | Potassium-containing amphoacetate and betaine surfactants |
| KR102362047B1 (en) | 2017-03-09 | 2022-02-11 | 벨베데레 폴리어 엘엘씨 | Post-emergence herbicide |
| WO2019149670A1 (en) | 2018-02-01 | 2019-08-08 | Nouryon Chemicals International B.V. | Alkyliminodipropionates for agricultural use |
| WO2020254095A1 (en) | 2019-06-17 | 2020-12-24 | Rhodia Operations | Agrochemical composition comprising particles of silicate and a fungicide |
| WO2020254855A1 (en) | 2019-06-17 | 2020-12-24 | Rhodia Poliamida E Especialidades S.A. | Method for treating plants using a composition comprising particles of silicate and of sulfate in a liquid carrier |
| WO2020254854A1 (en) | 2019-06-17 | 2020-12-24 | Rhodia Poliamida E Especialidades S.A. | Use of at least one silicate to increase the antioxidant activity of plants |
| WO2021007683A1 (en) | 2019-07-12 | 2021-01-21 | Rhodia Operations | Stable herbicidal compositions comprising amine oxide and betaine |
| US12439915B2 (en) * | 2019-09-20 | 2025-10-14 | Specialty Operations France | Stable herbicidal compositions comprising amine oxide and tertiary amine |
| WO2021069956A1 (en) | 2019-10-09 | 2021-04-15 | Rhodia Brasil S.A. | Agrochemical composition |
| EP4077584A1 (en) | 2019-12-19 | 2022-10-26 | Rhodia Operations | Method for treating a plant |
| CN114829540A (en) | 2019-12-19 | 2022-07-29 | 罗地亚经营管理公司 | Use of inorganic phosphors for increasing corn and soybean cultivation yield |
| CN114794099B (en) | 2021-01-19 | 2024-10-25 | 诺力昂化学品国际有限公司 | Nitrogen-containing surfactants for agriculture |
| WO2022268975A1 (en) | 2021-06-23 | 2022-12-29 | Rhodia Operations | Method for treating a plant |
| GB202117875D0 (en) * | 2021-11-16 | 2022-01-26 | Rhodia Operations | Choline-betaine based adjuvants for herbicides |
Family Cites Families (133)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3225074A (en) * | 1959-12-28 | 1965-12-21 | American Cyanamid Co | Betaines |
| GB1170927A (en) * | 1965-12-20 | 1969-11-19 | Ici Ltd | Herbicidal Compositions and their use |
| US3723357A (en) | 1970-11-16 | 1973-03-27 | Colgate Palmolive Co | Liquid detergent compositions |
| US4011388A (en) | 1974-07-02 | 1977-03-08 | E. I. Du Pont De Nemours And Company | Process for preparing emulsions by polymerization of aqueous monomer-polymer dispersions |
| US4117107A (en) | 1975-10-17 | 1978-09-26 | Noxell Corporation | Method and composition for improving oral hygiene |
| CA1052273A (en) | 1975-12-18 | 1979-04-10 | Edwin B. Michaels | Antimicrobial compositions |
| US4137191A (en) | 1977-02-14 | 1979-01-30 | Inolex Corporation | Low-irritant surfactant composition |
| FR2381813A1 (en) * | 1977-02-24 | 1978-09-22 | Oreal | FOAMING COMPOSITION FOR PRESSURIZED CONTAINER OF THE "AEROSOL BOMBE" TYPE |
| FR2398797B1 (en) * | 1977-07-26 | 1981-02-06 | Albright & Wilson | CONCENTRATED AQUEOUS SURFACTANT COMPOSITIONS |
| US4452732A (en) * | 1981-06-15 | 1984-06-05 | The Procter & Gamble Company | Shampoo compositions |
| US4477365A (en) | 1983-01-06 | 1984-10-16 | Miles Laboratories, Inc. | Caustic based aqueous cleaning composition |
| US5080809A (en) * | 1983-01-28 | 1992-01-14 | Phillips Petroleum Company | Polymers useful in the recovery and processing of natural resources |
| US4703797A (en) * | 1983-12-28 | 1987-11-03 | Cities Service Co. | Sweep improvement in enhanced oil recovery |
| US4585846A (en) | 1985-01-02 | 1986-04-29 | Exxon Research And Engineering Co. | Cyclopolymerizable sulfobetaine monomer |
| US4708998A (en) | 1985-01-02 | 1987-11-24 | Exxon Research And Engineering Company | Cyclopolymerizable sulfobetaine monomer |
| US5153289A (en) | 1985-01-02 | 1992-10-06 | Exxon Research And Engineering Company | Betaine copolymers-viscosifiers for water and brine |
| US4607076A (en) | 1985-01-02 | 1986-08-19 | Exxon Research And Engineering Co. | Betaine copolymers-viscosifiers for water and brine |
| US4650848A (en) * | 1985-12-30 | 1987-03-17 | Exxon Research & Engineering Company | Terpolymers of acrylamide, alkylacrylamide and betaine monomers |
| US4882405A (en) * | 1985-12-30 | 1989-11-21 | Exxon Research And Engineering Company | Terpolymers of acrylamide, alkylacrylamide and betaine monomers |
| US4742135A (en) * | 1985-12-30 | 1988-05-03 | Exxon Research And Engineering Company | Terpolymers of acrylamide, alkylacrylamide and betaine monomers |
| US4822847A (en) * | 1986-01-27 | 1989-04-18 | Exxon Research And Engineering Company | Method of increasing viscosity of an aqueous solution with a sulfo betaine polymer |
| US4835234A (en) | 1986-09-08 | 1989-05-30 | Exxon Research And Engineering Company | Hydrophobically functionalized cationic polymers |
| US4831092A (en) * | 1986-09-08 | 1989-05-16 | Exxon Research And Engineering Company | Micellar process for preparing hydrophobically functionalized cationic polymers (C-2114) |
| US4788247A (en) | 1986-09-15 | 1988-11-29 | Exxon Research And Engineering Company | Terpolymers of acrylamide, alkyl polyetheroxyacrylate and betaine monomers |
| JPH072608B2 (en) | 1986-12-04 | 1995-01-18 | モンサント コンパニ− | Aqueous concentrated herbicide formulation |
| US4996045A (en) | 1988-11-16 | 1991-02-26 | National Starch And Chemical Investment Holding Corporation | Hair fixative compositions containing alpha-aminomethylene phosphonate betaines |
| CA2004812A1 (en) | 1988-12-12 | 1990-06-12 | Michael Massaro | Detergent composition comprising betaine and ether sulphate |
| NZ231897A (en) * | 1988-12-30 | 1992-09-25 | Monsanto Co | Dry water-soluble granular composition comprising glyphosate and a liquid surfactant |
| GB2243846B (en) | 1990-03-26 | 1993-05-12 | Albright & Wilson | Flame retardant treatment of fabrics |
| FR2662053B1 (en) * | 1990-05-21 | 1992-08-07 | Rhone Poulenc Agrochimie | HERBICIDE SOLUTIONS BASED ON N-PHOSPHONOMETHYLGLYCIN. |
| EP0483095A3 (en) | 1990-10-04 | 1992-05-13 | Monsanto Company | Improved formulations |
| ATE150254T1 (en) | 1991-01-24 | 1997-04-15 | Monsanto Co | FORMULATIONS OF GLYPHOSATES |
| WO1992014907A1 (en) | 1991-02-22 | 1992-09-03 | The Western Company Of North America | Slurried polymer foam system and method for the use thereof |
| FR2675014B1 (en) | 1991-04-09 | 1993-06-25 | Rhone Poulenc Chimie | AQUEOUS COMPOSITIONS OF PHYTOSANITARY ACTIVE MATERIALS COMPRISING SUCROGLYCERIDES. |
| US5258358A (en) * | 1991-04-27 | 1993-11-02 | Hoechst Aktiengesellschaft | Liquid herbicidal compositions containing glufosinate and an alkyl polyglycoside |
| US5164120A (en) * | 1991-05-10 | 1992-11-17 | Ethyl Corporation | Surfactant mixtures |
| AU655282B2 (en) | 1991-06-14 | 1994-12-15 | Rhone-Poulenc Agro | New aqueous formulations |
| US6284854B1 (en) | 1991-07-05 | 2001-09-04 | Biccompatibles Limited | Polymeric surface coatings |
| ATE196482T1 (en) | 1991-07-05 | 2000-10-15 | Biocompatibles Ltd | POLYMERIC SURFACE COATING COMPOSITIONS |
| US5258359A (en) | 1991-08-02 | 1993-11-02 | Monsanto Company | Glyphosant-containing herbicidal compositions comprising acetylenic diol rainfastness enhancing agents |
| DE4207386C2 (en) * | 1992-03-09 | 1997-02-13 | Goldschmidt Ag Th | Aqueous liquid solution of a betaine containing at least 40% by weight of solids |
| DE4211190A1 (en) | 1992-04-03 | 1993-10-07 | Hoechst Ag | Process for the preparation of aqueous betaine solutions |
| US5290482A (en) | 1992-06-01 | 1994-03-01 | Colgate-Palmolive Company | Surfactant compositions comprising betaine/cocoamide complexes and method of making the same |
| US5338793A (en) | 1992-06-02 | 1994-08-16 | The Gillette Company | Erasable ink |
| MY111437A (en) | 1992-07-31 | 2000-05-31 | Monsanto Co | Improved glyphosate herbicide formulation. |
| US5439317A (en) | 1992-10-08 | 1995-08-08 | Pb-Kbb Inc. | Method of handling solid particles |
| KR960700332A (en) | 1993-01-12 | 1996-01-19 | 웨인 씨. 제쉬크 | Hand Wash Cleaner (DISHWASHING DETERGENT) |
| US5385206A (en) * | 1993-01-21 | 1995-01-31 | Clearwater, Inc. | Iterated foam process and composition for well treatment |
| US5747416A (en) * | 1993-07-08 | 1998-05-05 | Mcardle; Blaise | Herbicidal and insecticidal protein-polysaccharide delivery compositions and methods for controlling plant and insect populations |
| US5912209A (en) | 1993-12-17 | 1999-06-15 | Monsanto Company | Surfactants providing enhanced efficacy and/or rainfastness to glyphosate formulations |
| GB9412722D0 (en) | 1994-06-24 | 1994-08-17 | Zeneca Ltd | Herbicidal composition |
| US5580856A (en) | 1994-07-15 | 1996-12-03 | Prestrelski; Steven J. | Formulation of a reconstituted protein, and method and kit for the production thereof |
| US5551516A (en) * | 1995-02-17 | 1996-09-03 | Dowell, A Division Of Schlumberger Technology Corporation | Hydraulic fracturing process and compositions |
| MY114016A (en) | 1995-06-27 | 2002-07-31 | Kao Corp | Liquid enhancer composition for amino acid series herbicides |
| ES2195003T3 (en) | 1995-08-04 | 2003-12-01 | Reckitt Benckiser Inc | CLEANING AND / OR DISINFECTANT COMPOSITIONS OF OPALCENT TYPE FOR HARD SURFACES. |
| US5700760A (en) * | 1996-04-03 | 1997-12-23 | Albemarle Corporation | Herbicidal and plant growth regulant compositions and their use |
| US5710103A (en) | 1996-04-03 | 1998-01-20 | Albemarle Corporation | Glyphosate compositions comprising hydrocarbyl dimethyl amine oxide and quaternary ammonium halide |
| US5874394A (en) * | 1996-04-08 | 1999-02-23 | Colgate Palmolive Company | Light duty liquid cleaning compositions containing a monoalkyl phosphate ester |
| GB9612067D0 (en) | 1996-06-10 | 1996-08-14 | Smithkline Beecham Plc | Composition |
| US5703016A (en) | 1996-09-30 | 1997-12-30 | Albemarle Corporation | Surfactant composition for use with glyphosate comprising dimethyl amine oxide, polyethoxylated alcohol, and pyridinium halide |
| CA2269726A1 (en) * | 1996-10-25 | 1998-04-30 | Monsanto Company | Composition and method for treating plants with exogenous chemicals |
| US20020161108A1 (en) | 2000-03-09 | 2002-10-31 | Stepan Company, A Corporation Of The State Of Delaware | Emulsion polymerization process utilizing ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids |
| US6258859B1 (en) * | 1997-06-10 | 2001-07-10 | Rhodia, Inc. | Viscoelastic surfactant fluids and related methods of use |
| AU8401998A (en) | 1997-07-15 | 1999-02-10 | Rhodia Chimie | Method for producing polymers using micellar polymerization |
| WO1999004635A1 (en) | 1997-07-22 | 1999-02-04 | Monsanto Company | High-loaded ammonium glyphosate formulations |
| US5897699A (en) | 1997-07-23 | 1999-04-27 | Halliburton Energy Services, Inc. | Foamed well cement compositions, additives and methods |
| US6302209B1 (en) | 1997-09-10 | 2001-10-16 | Bj Services Company | Surfactant compositions and uses therefor |
| DE19742285C1 (en) | 1997-09-25 | 1999-04-29 | Henkel Kgaa | Use of unsaturated betaine surfactants as thickeners |
| JP2932377B2 (en) | 1997-10-31 | 1999-08-09 | 川研ファインケミカル株式会社 | Liquid detergent thickening method |
| US6036638A (en) * | 1997-11-04 | 2000-03-14 | Nwawka; Chudi C. | Vaginal sleeve |
| US5877143A (en) | 1997-11-20 | 1999-03-02 | Colgate-Palmolive Co. | Composition containing a lamellar liquid crystalline phase which comprises betaines and amine oxides |
| US6432884B1 (en) * | 1997-12-08 | 2002-08-13 | Cognis Corporation | Agricultural adjuvant |
| HUP0100862A3 (en) | 1998-03-09 | 2002-03-28 | Monsanto Technology Llc St Louis | Concentrate herbicidal composition and use thereof |
| US6127318A (en) * | 1998-04-03 | 2000-10-03 | Monsanto Company | Combination of glyphosate and a triazolinone herbicide |
| US5985798A (en) | 1998-06-04 | 1999-11-16 | Hampshire Chemical Corp. | N-acyl sarcosinates as glyphosate adjuvants |
| JPH11349826A (en) | 1998-06-09 | 1999-12-21 | Nippon Shokubai Co Ltd | Production of polymeric absorbent |
| GB9823752D0 (en) | 1998-10-30 | 1998-12-23 | Allied Colloids Ltd | Compositions comprising anti-drift agents and processes and methods for their use |
| ES2200589T3 (en) * | 1998-12-23 | 2004-03-01 | Huntsman International Llc | HERBICIDE AND CONCENTRATED COMPOSITIONS OF TENSIOACTIVE AGENTS. |
| US6432878B1 (en) | 1999-01-15 | 2002-08-13 | Cognis Corporation | Adjuvant composition |
| FR2792546B1 (en) * | 1999-04-26 | 2003-01-03 | Rhodia Chimie Sa | SOLID COMPOSITION INCLUDING AT LEAST ONE LOW MELTING-POINT SURFACTANT |
| US6364926B1 (en) * | 1999-04-30 | 2002-04-02 | Precision Laboratories, Inc. | Concentrated liquid adjuvant and fertilizer |
| AUPQ017699A0 (en) * | 1999-05-05 | 1999-05-27 | Victorian Chemicals International Pty Ltd | Agrochemical composition |
| AUPQ017599A0 (en) | 1999-05-05 | 1999-05-27 | Victorian Chemicals International Pty Ltd | Adjuvant composition for chemicals used in agriculture |
| DE19930031A1 (en) | 1999-06-30 | 2001-01-04 | Sueddeutsche Kalkstickstoff | Sulfobetaine-based terpolymers used as thickeners for aqueous salt solutions, especially oilfield brines, contain optionally substituted acrylamide, hydroxy-alkyl (meth)acrylate and sulfobetaine monomer units |
| AU6373200A (en) | 1999-07-27 | 2001-02-13 | Rhodia Inc. | Hybrid ionic phosphorus surfactant adjuvants for bioactive compositions |
| GB9917976D0 (en) * | 1999-07-31 | 1999-09-29 | Albright & Wilson Uk Ltd | Herbicidal compositions |
| US6210476B1 (en) * | 1999-09-07 | 2001-04-03 | Halliburton Energy Services, Inc. | Foamed cement compositions and methods |
| US6908882B1 (en) | 1999-09-09 | 2005-06-21 | Monsanto Company | Enhanced method of killing weeds with glyphosate herbicide |
| US6451731B1 (en) * | 1999-09-10 | 2002-09-17 | Monsanto Company | Stable concentrated pesticidal suspension |
| WO2001026463A1 (en) | 1999-10-13 | 2001-04-19 | Nufarm Limited | Adjuvant for a herbicidal composition |
| EP1220610A4 (en) | 1999-10-13 | 2003-01-22 | Nufarm Ltd | Herbicidal composition and adjuvant |
| US6417268B1 (en) * | 1999-12-06 | 2002-07-09 | Hercules Incorporated | Method for making hydrophobically associative polymers, methods of use and compositions |
| US6992045B2 (en) | 2000-05-19 | 2006-01-31 | Monsanto Technology Llc | Pesticide compositions containing oxalic acid |
| US7135437B2 (en) * | 2000-05-19 | 2006-11-14 | Monsanto Technology Llc | Stable liquid pesticide compositions |
| MY158895A (en) | 2000-05-19 | 2016-11-30 | Monsanto Technology Llc | Potassium glyphosate formulations |
| US6703351B2 (en) * | 2000-06-13 | 2004-03-09 | Baker Hughes Incorporated | Water-based drilling fluids using latex additives |
| US6376566B1 (en) * | 2000-06-14 | 2002-04-23 | Rhodia Inc. | Agricultural foam marker compositions and use thereof |
| US6369122B1 (en) | 2000-06-14 | 2002-04-09 | Rhodia Inc. | Agricultural foam marker compositions and use thereof |
| DE10036002A1 (en) | 2000-07-25 | 2002-02-14 | Aventis Cropscience Gmbh | Herbicidal agents |
| US6566408B1 (en) | 2000-08-01 | 2003-05-20 | Rhodia, Inc. | Aqueous surfactant compositions of monoalkyl phosphate ester salts and amphoteric surfactants |
| GB0023912D0 (en) | 2000-09-29 | 2000-11-15 | Zeneca Ltd | Agrochemical Composition |
| US20020187917A1 (en) | 2001-05-14 | 2002-12-12 | Virginia Lazarowitz | High-foaming non-anionic surfactant compositions |
| AUPR682201A0 (en) * | 2001-08-03 | 2001-08-30 | Nufarm Limited | Glyphosate composition |
| US6642178B2 (en) * | 2001-11-14 | 2003-11-04 | North Dakota State University | Adjuvant blend for enhancing efficacy of pesticides |
| CN1599633B (en) | 2001-12-07 | 2010-05-12 | 苏尔贝格斯堪的纳维亚股份有限公司 | Aqueous foaming composition |
| US8236730B2 (en) | 2002-01-29 | 2012-08-07 | Rhodia Chimie | Aqueous herbicidal concentrate comprising a betaine type surfactant |
| US20030158042A1 (en) * | 2002-01-29 | 2003-08-21 | Valerio Bramati | Concentrated aqueous phytopathological formulation comprising a herbicide and a betaine type surfactant |
| US6645914B1 (en) | 2002-05-01 | 2003-11-11 | Ndsu-Research Foundation | Surfactant-ammonium sulfate adjuvant composition for enhancing efficacy of herbicides |
| US6579514B1 (en) * | 2002-05-08 | 2003-06-17 | David M. Hall | Anti infective periodontic compositions |
| US7883715B2 (en) * | 2002-08-31 | 2011-02-08 | Monsanto Technology Llc | Pesticide compositions containing dicarboxylic acids |
| US20040121917A1 (en) | 2002-12-20 | 2004-06-24 | Pakulski Marek K | Synergistic mixtures containing an amino acid derivative and a method of using the same to foam brines |
| DE10325197A1 (en) | 2003-06-04 | 2004-12-23 | Clariant Gmbh | Preparations containing quaternary ammonium compounds and anionic surfactants |
| DE10325199A1 (en) | 2003-06-04 | 2004-12-23 | Clariant Gmbh | Preparations containing amine oxides and anionic surfactants |
| US20050003965A1 (en) | 2003-07-01 | 2005-01-06 | Zhijun Xiao | Hydraulic fracturing method |
| US7148184B2 (en) * | 2003-07-22 | 2006-12-12 | Schlumberger Technology Corporation | Self-diverting foamed system |
| MXPA06001389A (en) * | 2003-08-04 | 2006-05-15 | Dow Agrosciences Llc | High-strength, low viscosity herbicidal formulations of glyphosate. |
| DE10357682A1 (en) | 2003-12-10 | 2005-07-07 | Goldschmidt Ag | Biocide-effective combination for agricultural applications |
| CA2554335A1 (en) | 2004-01-27 | 2005-08-04 | Merck Patent Gesellschaft Mit Beschraenkter Haftung | Use of statistical copolymers |
| DE102004004209A1 (en) | 2004-01-27 | 2005-08-18 | Merck Patent Gmbh | Use of random copolymer with hydrophobic and hydrophilic groups in different structural units as emulsifier is useful for producing polymer-modified nanoparticles, e.g. of silica, silver or metal sulfide or carbonate for use in polymer |
| US7191834B2 (en) * | 2004-09-22 | 2007-03-20 | Halliburton Energy Services, Inc. | Foamed cement compositions and associated methods of use |
| JP2006117650A (en) | 2004-09-27 | 2006-05-11 | Kao Corp | Herbicidal composition |
| AU2005321478B2 (en) * | 2004-12-30 | 2009-11-05 | Specialty Operations France | Herbicidal composition comprising an aminophosphate or aminophosphonate salt and a betaine |
| NZ564145A (en) | 2005-05-17 | 2009-12-24 | Rhodia | Agricultural adjuvant compositions comprising a betaine surfactant and glycerol, herbicide compositions, and methods for using such compositions |
| CN100382704C (en) | 2005-07-01 | 2008-04-23 | 叶允敏 | Environmental-protection quick thermo-osmosis dual-contact weedicide |
| US20090018018A1 (en) * | 2005-11-10 | 2009-01-15 | Rhodia Operations | Herbicidal composition comprising aminophosphate or aminophosphonate potassium salt |
| NZ567994A (en) | 2005-11-14 | 2012-03-30 | Rhodia | Surfactant is sodium alkyl ether sulfate in agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions |
| WO2008066611A2 (en) | 2006-10-16 | 2008-06-05 | Rhodia Inc. | Agricultural adjuvant compositions. pesticide compositions. and methods for using such compositions |
| FR2913351B1 (en) | 2007-03-08 | 2010-11-26 | Rhodia Recherches Et Tech | USE OF BETAINE AS A DRAINAGE REDUCTION AGENT FOR FOAM |
| FR2913350B1 (en) * | 2007-03-08 | 2010-05-21 | Rhodia Recherches & Tech | USE OF BETAINE AS FOAMING AGENT AND FOAM DRAIN REDUCTION AGENT |
| FR2914647B1 (en) | 2007-04-05 | 2011-10-21 | Rhodia Recherches Et Tech | COPOLYMER COMPRISING BETAINIC UNITS AND HYDROPHOBIC AND / OR AMPHIPHILIC UNITS, PREPARATION METHOD, AND USES. |
| CN101932236A (en) | 2007-11-07 | 2010-12-29 | 罗地亚管理公司 | Herbicidal composition comprising an aminophosphate or aminophosphonate salt and a viscosity-reducing agent |
| US8748344B2 (en) | 2009-07-14 | 2014-06-10 | Rhodia Operations | Agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions |
| US8841235B2 (en) | 2010-08-10 | 2014-09-23 | Rhodia Operations | Agricultural pesticide compositions |
-
2005
- 2005-12-30 AU AU2005321478A patent/AU2005321478B2/en not_active Expired
- 2005-12-30 PT PT58434002T patent/PT1835808E/en unknown
- 2005-12-30 CA CA2591052A patent/CA2591052C/en not_active Expired - Lifetime
- 2005-12-30 US US11/794,297 patent/US20080312083A1/en not_active Abandoned
- 2005-12-30 US US11/794,299 patent/US9045720B2/en active Active
- 2005-12-30 DK DK05843400.2T patent/DK1835808T3/en active
- 2005-12-30 RU RU2007128937/04A patent/RU2369097C2/en active
- 2005-12-30 MX MX2007008012A patent/MX2007008012A/en active IP Right Grant
- 2005-12-30 ES ES05843400.2T patent/ES2445033T3/en not_active Expired - Lifetime
- 2005-12-30 EP EP05849076.4A patent/EP1830652B1/en not_active Expired - Lifetime
- 2005-12-30 WO PCT/EP2005/014146 patent/WO2006069794A2/en not_active Ceased
- 2005-12-30 NZ NZ556091A patent/NZ556091A/en unknown
- 2005-12-30 EP EP05843400.2A patent/EP1835808B1/en not_active Expired - Lifetime
- 2005-12-30 WO PCT/EP2005/014131 patent/WO2006069791A1/en not_active Ceased
- 2005-12-30 BR BRPI0519316A patent/BRPI0519316B8/en active IP Right Grant
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2006
- 2006-01-02 AR ARP060100003A patent/AR052188A1/en active IP Right Grant
- 2006-01-02 AR ARP060100002A patent/AR052187A1/en not_active Application Discontinuation
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- 2007-06-18 IL IL184030A patent/IL184030A/en active IP Right Grant
- 2007-07-26 ZA ZA200706187A patent/ZA200706187B/en unknown
-
2015
- 2015-11-09 US US14/936,192 patent/US20160057997A1/en not_active Abandoned
-
2019
- 2019-11-21 US US16/690,415 patent/US20200085040A1/en not_active Abandoned
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| IL184030A (en) | 2016-10-31 |
| US9045720B2 (en) | 2015-06-02 |
| US20080103047A1 (en) | 2008-05-01 |
| AU2005321478A1 (en) | 2006-07-06 |
| RU2369097C2 (en) | 2009-10-10 |
| WO2006069794A2 (en) | 2006-07-06 |
| EP1830652A2 (en) | 2007-09-12 |
| EP1835808A1 (en) | 2007-09-26 |
| AU2005321478B2 (en) | 2009-11-05 |
| MX2007008012A (en) | 2007-08-23 |
| DK1835808T3 (en) | 2014-02-10 |
| US20200085040A1 (en) | 2020-03-19 |
| EP1835808B1 (en) | 2013-11-06 |
| CA2591052C (en) | 2011-08-16 |
| AR052187A1 (en) | 2007-03-07 |
| US20080312083A1 (en) | 2008-12-18 |
| BRPI0519316B8 (en) | 2021-06-29 |
| WO2006069791A1 (en) | 2006-07-06 |
| ES2445033T3 (en) | 2014-02-27 |
| US20160057997A1 (en) | 2016-03-03 |
| WO2006069794A3 (en) | 2006-10-12 |
| BRPI0519316A2 (en) | 2009-01-13 |
| NZ556091A (en) | 2009-09-25 |
| ZA200706187B (en) | 2008-09-25 |
| RU2007128937A (en) | 2009-02-10 |
| IL184030A0 (en) | 2007-10-31 |
| EP1830652B1 (en) | 2013-11-06 |
| AR052188A1 (en) | 2007-03-07 |
| CA2591052A1 (en) | 2006-07-06 |
| PT1835808E (en) | 2014-02-11 |
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